Canonical Allele Identifier: CA419200420

Gene: COL11A1

Linked Data

• MyVariant Identifiers: chr1:g.103444646T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102979090T>C , CM000663.2:g.102979090T>C	GRCh38
NC_000001.10:g.103444646T>C , CM000663.1:g.103444646T>C	GRCh37
NC_000001.9:g.103217234T>C	NCBI36
NG_008033.1:g.134407A>G
NG_008033.2:g.134407A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2625A>G MANE Select	ENSP00000359114.3:p.Lys875=
ENST00000353414.8:c.2508A>G	ENSP00000302551.6:p.Lys836=
ENST00000358392.6:c.2661A>G	ENSP00000351163.2:p.Lys887=
ENST00000370096.7:c.2625A>G	ENSP00000359114.3:p.Lys875=
ENST00000512756.5:c.2277A>G	ENSP00000426533.1:p.Lys759=
ENST00000635193.1:c.1959A>G
NM_001190709.1:c.2508A>G	NP_001177638.1:p.Lys836=
NM_001854.3:c.2625A>G	NP_001845.3:p.Lys875=
NM_080629.2:c.2661A>G	NP_542196.2:p.Lys887=
NM_080630.3:c.2277A>G	NP_542197.3:p.Lys759=
XM_011540719.1:c.2625A>G	XP_011539021.1:p.Lys875=
XM_011540720.1:c.858A>G	XP_011539022.1:p.Lys286=
XM_011540721.1:c.213A>G	XP_011539023.1:p.Lys71=
XR_946545.1:n.3039A>G
NR_134980.1:n.2959A>G
XM_017000334.1:c.2778A>G	XP_016855823.1:p.Lys926=
XM_017000335.1:c.2772A>G	XP_016855824.1:p.Lys924=
XM_017000336.1:c.2778A>G	XP_016855825.1:p.Lys926=
XM_017000337.1:c.1176A>G	XP_016855826.1:p.Lys392=
NM_001854.4:c.2625A>G MANE Select	NP_001845.3:p.Lys875=
NM_080630.4:c.2277A>G	NP_542197.3:p.Lys759=
NR_134980.2:n.2985A>G
NM_001190709.2:c.2508A>G	NP_001177638.1:p.Lys836=
NM_080629.3:c.2661A>G	NP_542196.2:p.Lys887=